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Sorting out the Diagnostics

Sorting out the Diagnostics. Ed Marino, PA-C Porter Adventist Hospital Liver Transplant Services Denver, CO. Acknowledgements. Thanks to the organizers for my invitation Especially Corinna Dan, RN, MPH Staff at Hepatitis Foundation International

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Sorting out the Diagnostics

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  1. Sorting out the Diagnostics Ed Marino, PA-C Porter Adventist Hospital Liver Transplant Services Denver, CO

  2. Acknowledgements • Thanks to the organizers for my invitation • Especially Corinna Dan, RN, MPH • Staff at Hepatitis Foundation International • Staff at Porter Hospital Liver Transplant Service for allowing me time away for this

  3. Educational Objectives • Review the most common liver lab tests • Determine true liver synthetic function • Review viral hepatitis lab values • Discuss follow up for above labs

  4. Hepatic Physiology • Liver: • Largest solid organ in the body • Performs over 500 chemical processes • Produces over 160 different proteins • Makes clotting factors for the blood • Stores & releases sugar as glycogen • Metabolizes, detoxifies, synthesizes

  5. The Anatomy of the Liver

  6. CT

  7. Liver Histology

  8. Defining Terms • Hepatitis: refers to any swelling, inflammation, or irritation of the liver • Over 100 causes including: • Viruses, alcohol, enzyme deficiencies • Iron or copper overload, microvesicular fat • Genetic disorders, licit & illicit drugs, toxins • Hypotension (shock liver / reperfusion)

  9. Defining Terms • Inflammation that lasts long enough will create fibrosis • Extreme fibrosis is called cirrhosis • Cirrhosis can be either compensated or decompensated • Compensated cirrhosis can be subtle • Decompensated cirrhosis is more obvious

  10. Normal Liver

  11. Cirrhotic Liver

  12. Defining Terms • Normal Lab Values: 95% of normal, asymptomatic patients have numbers in this range on a “bell shaped curve” • Abnormal Labs: By definition, 2.5% of normal patients have lab values either above or below the “normal” range

  13. Liver “Function” Tests • ALT: alanine aminotransferase (SGPT) • AST: aspartate aminotransferase (SGOT) • Alkaline Phosphatase & Bilirubin • Known as LFT’s (but they’re really not)

  14. Liver Synthetic Function • Total Protein and serum albumin • Total Bilirubin • Prothrombin Time (PT / INR) • These are “true” tests of liver function

  15. Traditional LFT’s • ALT: • Found primarily in hepatocytes • Released when cells are hurt or destroyed • Normal levels depend on the reference range which actually differs lab to lab • Considered normal between 5-40 U/L • Probably should be half of this (5-20?)

  16. Traditional LFT’s • AST: • Found in many sources, including liver, heart, muscle, intestine, pancreas • Not very specific for liver disease • Often follows ALT to a degree • Elevated 2 or 3:1 (vs. ALT) in alcoholics • Normal range: 8-20 U/L

  17. Traditional LFT’s • Alkaline Phosphatase: • Found in liver (especially biliary tract), bones, intestines, & placenta • “Fractionated” or “isoenzymes” to source • Liver AP rises with obstruction or infiltrative diseases (i.e., stones or tumors) • Normal range: 20-70 U/L

  18. Traditional LFT’s • Bilirubin: two primary sources • Indirect (unconjugated): old red cells, removed by the spleen, sent to the liver • Liver “adds” glucuronic acid, making these cells water soluble for excretion; now called direct (or conjugated) • Normal range: less than 0.8 mg/dL

  19. Traditional LFT’s • Bilirubin: Indirect and direct • Direct (conjugated): Total bilirubin includes both direct and indirect types • Excreted in the bile, down the common bile duct, into the small intestine • Normal range: 0.3 – 1.0 mg/ dL

  20. Patterns of Abnormal • Elevations in ALT & AST only: suggests cellular injury • Elevations in Alk Phos & Bilirubin: suggests cholestasis or obstruction • Mixed pattern: ALT, AST, AP & Bili: probably the most common scenario

  21. Patterns of Abnormal • Consider degree of elevation: • Very high ALT and AST usually only come from a couple of sources: • Acute viral hepatitis (A,B,C, HSV) • Acetominophen toxicity / overdose • “Shock Liver”; cardiac or surgical event? • Most other items don’t cause huge levels

  22. Viral Hepatitides • Hepatitis A, B, C, D, E, G • Cytomeglovirus (CMV) • Herpes Virus (HSV) • West Nile Virus (WNV)

  23. Viral Hepatitides • Hepatitis A (HAV): • Food, water borne; heat labile • Fecal - oral contamination; contagious • Usually self limited, lasting days to weeks • 99% spontaneous recovery, no treatment • Tests: HAV IgM antibody = acute infection • HAV total antibody (IgM & IgG) = exposure only, could be post infection or vaccination

  24. Viral Hepatitides • Hepatitis B (HBV): • Blood, semen, saliva, vaginal secretions • Highly contagious; sexually transmitted • 90-95% self limited over 6 months • Chronic infection: >6 months • DNA virus: incorporates into host with chronic infection

  25. Viral Hepatitides • HBV Lab Tests: • HBV s Ag: surface antigen; + infection • HBV s Ab: surface antibody; - infection • HBV c Ab: core antibody IgM, IgG; only + with infection, not vaccination • HBV e Ag: envelope antigen; if + actively replicating virus • HBV DNA: actual viral load in blood

  26. Viral Hepatitides • Hepatitis C (HCV): • Blood borne, not in food or water; not highly sexually transmitted* • Not highly contagious • 20% self clearing; 80% chronicity • RNA virus: does not incorporate into host • Can cause HCC; #1 cause of transplant

  27. Viral Hepatitides • HCV Ab: + means past exposure; can take 3-6 months to form; not found if acute • RIBA / ELISA: used to confirm Ab; + rules out false positives • HCV PCR RNA: confirms actual viral presence in blood; can be +/- or a viral count (qualitative vs. quantitative) • HCV Genotype: there are at least six (6) different (geno)types of HCV virus

  28. Viral Hepatitides • HCV Genotypes: different mutations of same virus (different branches, same tree) • Can vary by global geography • Not predicative of damage or symptoms • Can predict response to treatment • Can be used to determine who is the best treatment candidate • G1 & 4: most stubborn; G2 & 3: most responsive; G5 & 6: most rare

  29. Evaluation Strategy • Hepatocellular Injury: • Liver biopsy remains the “Gold Standard” for diagnosis • Biopsy is second only to a good history • If a biopsy is obtained, you’ll need a very experienced pathologist to read it • Consider sending it out if your local expertise is suspect

  30. Evaluation Strategy • Advanced Imaging: • If RUQ US is questionable, and you’re looking at a mixed picture: • Consider an MRCP: non-invasive, sensitive for ductal dilation (CBD, pancreatic ducts). Diagnostic, but non-therapeutic. • ERCP: Therapeutic, risk of pancreatitis, not available everywhere

  31. Spider Angiomata

  32. Spider Nevi

  33. Nail Clubbing

  34. Dupuytren's Contracture

  35. Ascites

  36. Jaundice or Scleral Icterus

  37. Evaluation Strategy • Clinical Pearls: • Acute hepatitis panels never consider acute HCV. If you have a IVDA pt, consider an HCV PCR for acute hepatitis C. HIV? • Consider celiac sprue for abnormal LFT’s, especially if you get a vague history of dyspepsia. Order TTG (tissue transglutaminase antibodies) with AGA (anti gliadin antibodies).

  38. Summary • Liver tests are numerous and somewhat confusing • Not all liver disease is associated with abnormal test results • Some of the worst liver disease has relatively normal appearing LFT’s and can only be noticed with a look at synthetic functions

  39. Summary • All abnormal liver tests should be investigated • Referral to an expert is absolutely needed • Liver biopsy is the “Gold Standard” for diagnosis • Family histories of liver disease should be noted: “.…my grandmother died of cirrhosis, but she never drank….”

  40. Thank You! • My contact information: Ed Marino, PA-C Porter Hospital Liver Transplant Service 2535 S. Downing St., Suite #380 Denver, CO 80210 edwardmarino@centura.org Wk. 303.778.5797 Fax 303.778.5205

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